{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["An AY"],"funding":["NIAID NIH HHS"],"pagination":["105411"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11663757"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["110"],"pubmed_abstract":["<h4>Background</h4>Neonatal sepsis is a deadly disease with non-specific clinical signs, delaying diagnosis and treatment. There remains a need for early biomarkers to facilitate timely intervention. Our objective was to identify neonatal sepsis gene expression biomarkers that could predict sepsis at birth, prior to clinical presentation.<h4>Methods</h4>Among 720 initially healthy full-term neonates in two hospitals (The Gambia, West Africa), we identified 21 newborns who were later hospitalized for sepsis in the first 28 days of life, split into early-onset sepsis (EOS, onset ≤7 days of life) and late-onset sepsis (LOS, onset 8-28 days of life), 12 neonates later hospitalized for localized infection without evidence of systemic involvement, and 33 matched control neonates who remained hea"],"journal":["EBioMedicine"],"pubmed_title":["Predictive gene expression signature diagnoses neonatal sepsis before clinical presentation."],"pmcid":["PMC11663757"],"funding_grant_id":["K08 AI168487"],"pubmed_authors":["Amenyogbe N","Matlam JP","Rao S","Martino D","Huang J","Parker EPK","Larsen K","Ford R","Burnell K","Golding CN","Dibbasey T","Ndure J","van den Biggelaar AHJ","Wariri O","Njie-Jobe J","Fatou B","Bennike TB","Vo D","Odumade OA","Ben-Othman R","Chen V","Masiria G","Dhillon BK","Kirarock W","Palma P","Diray-Arce J","He D","Ozonoff A","Chen J","Cooney M","Idoko OT","Dibassey T","Francis F","Sanchez-Schmitz G","Darboe A","Plotkin A","An AY","Sanca L","Syphurs C","van Haren SD","Imam A","Smolen KK","Checkervarty A","Kraft K","Pak J","Lee AH","Bjerregaard-Andersen M","Pettengill MA","Montante S","McEnaney K","Levy O","Blimkie TM","Karoly ME","Richmond PC","Angelidou A","A","Kollmann TR","Steen H","Strandmark J","Liu M","Pomat WS","Blimkie T","Hoch A","Acton E","M","Brook B","Cai B","Hinshaw SH","Marchant A","Lasky-Su J","Vignolo S","Schaltz-Buchholzer F","Kampmann B","Falsafi R","Saleu G","Tebbutt SJ","EPIC Consortium","Shannon CP","Bennike T","Harbeson DJ","Bao W","Singh A","Malek M","Roberts E","Smith M","Hancock REW","Varankovich N","McLoughlin C","Liu A","Martino DJ","Nguyen A","Morrocchi E","Brinkman RR","Cox M"],"additional_accession":[]},"is_claimable":false,"name":"Predictive gene expression signature diagnoses neonatal sepsis before clinical presentation.","description":"<h4>Background</h4>Neonatal sepsis is a deadly disease with non-specific clinical signs, delaying diagnosis and treatment. There remains a need for early biomarkers to facilitate timely intervention. Our objective was to identify neonatal sepsis gene expression biomarkers that could predict sepsis at birth, prior to clinical presentation.<h4>Methods</h4>Among 720 initially healthy full-term neonates in two hospitals (The Gambia, West Africa), we identified 21 newborns who were later hospitalized for sepsis in the first 28 days of life, split into early-onset sepsis (EOS, onset ≤7 days of life) and late-onset sepsis (LOS, onset 8-28 days of life), 12 neonates later hospitalized for localized infection without evidence of systemic involvement, and 33 matched control neonates who remained hea","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Dec","modification":"2026-04-08T19:49:03.178Z","creation":"2025-04-03T23:14:04.174Z"},"accession":"S-EPMC11663757","cross_references":{"pubmed":["39472236"],"doi":["10.1016/j.ebiom.2024.105411"]}}